P7S (p.Pro7Ser) variant of ITGA2B (Integrin alpha-IIb)
P7S (p.Pro7Ser) in ITGA2B (Integrin alpha-IIb) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
P7S (p.Pro7Ser) variant details
- p.Pro7Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.61
- MetaSVM -0.41
- SIFT 0.07
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available